Dreger Peter, Brand Ronald, Michallet Mauricette
Department of Medicine V, University of Heidelberg, Heidelberg, Germany, and Department of Hematology, Hôpital Edouard Herriot, Lyon, France.
Semin Hematol. 2007 Oct;44(4):246-51. doi: 10.1053/j.seminhematol.2007.08.008.
Autologous stem cell transplantation (ASCT) has been intensively investigated for treatment of patients with chronic lymphocytic leukemia (CLL) during recent years. To assess the potential therapeutic value of ASCT for CLL, the present article aims at answering the following crucial questions: (1) Does ASCT have curative potential? (2) What is the therapeutic potential of ASCT in terms of disease control in relation to toxicity? (3) What is the role of ASCT in the current arsenal of CLL treatment modalities? Evidence from clinical and minimal residual disease (MRD) studies suggests that ASCT has curative potential in only a few patients, if any. Nevertheless, ASCT might be capable of prolonged disease control even in CLL with poor-risk features. Uncontrolled prospective studies have indicated the superiority of ASCT over alkylator and fludarabine monotherapy but not necessarily over purine analogue cyclophosphamide or antibody combinations. A significant risk of secondary neoplasms, in particular myelodysplasias, has to be taken into account. Therefore, ASCT cannot be considered as standard treatment for CLL and should be performed only in the context of clinical trials.
近年来,自体干细胞移植(ASCT)已被深入研究用于治疗慢性淋巴细胞白血病(CLL)患者。为评估ASCT对CLL的潜在治疗价值,本文旨在回答以下关键问题:(1)ASCT是否具有治愈潜力?(2)就疾病控制与毒性而言,ASCT的治疗潜力如何?(3)ASCT在当前CLL治疗模式体系中的作用是什么?临床和微小残留病(MRD)研究的证据表明,ASCT仅在极少数患者中(如果有的话)具有治愈潜力。然而,即使对于具有高危特征的CLL,ASCT也可能能够实现疾病的长期控制。非对照前瞻性研究表明,ASCT优于烷化剂和氟达拉滨单药治疗,但不一定优于嘌呤类似物环磷酰胺或抗体组合。必须考虑到继发肿瘤,尤其是骨髓发育异常的重大风险。因此,ASCT不能被视为CLL的标准治疗方法,仅应在临床试验的背景下进行。